Catalytic oxygen evolution reaction (OER) plays an important role in clean energy storage and conversion processes. Its transformation requires sequential intermediate valence change steps, which makes the dynamics of the catalytical cycle complicated.

Such a multi-redox mechanism involving multi-sites has implications to dictate the catalytic water oxidation. However, understanding the sequential dynamics of multi-steps in OER cycles on catalysts is still challenging.

Recently, a research group led by Profs. Li Can and Wang Xiuli from the Dalian Institute of Chemical 麻豆淫院ics (DICP) of the Chinese Academy of Sciences (CAS) has revealed sequential oxidation kinetics and determining roles of multi-cobalt active sites on Co₃O₄ catalyst for water oxidation.

The study was published in Journal of the American Chemical Society on Feb. 1.

The researchers employed quasi-operando transient absorption spectroscopy to study a typical photosensitization strategy, using Co₃O₄ nanoparticles as model catalysts.

They found that when OER was initiated from fast oxidation of surface Co²⁺ ions, both surface Co²⁺ and Co³⁺ ions were active sites of the multi-cobalt centers for water oxidation.

In the sequential kinetics (Co²⁺ 鈫� Co³⁺ 鈫� Co⁴⁺), the key characteristic was fast oxidation and slow consumption for all the cobalt species. Due to this characteristic, the Co⁴⁺ intermediate distribution played a determining role in OER activity and resulted in the slow overall OER kinetics.

"Our study deepens the understanding of the multi-redox kinetics of multi-active sites in OER catalytic cycle. It also sheds light on water oxidation mechanism and heterogeneous OER catalyst design," said Prof. Li.